APA (7th ed.) Citation

Teryutin, F. M., Pshennikova, V. G., Solovyev, A. V., Romanov, G. P., Fedorova, S. A., & Barashkov, N. A. (2024). Genotype–phenotype analysis of hearing function in patients with DFNB1A caused by the c.-23+1G>A splice site variant of the GJB2 gene (Cx26). PLoS ONE, 19(10), 1. https://doi.org/10.1371/journal.pone.0309439

Chicago Style (17th ed.) Citation

Teryutin, Fedor M., Vera G. Pshennikova, Aisen V. Solovyev, Georgii P. Romanov, Sardana A. Fedorova, and Nikolay A. Barashkov. "Genotype–phenotype Analysis of Hearing Function in Patients with DFNB1A Caused by the C.-23+1G>A Splice Site Variant of the GJB2 Gene (Cx26)." PLoS ONE 19, no. 10 (2024): 1. https://doi.org/10.1371/journal.pone.0309439.

MLA (9th ed.) Citation

Teryutin, Fedor M., et al. "Genotype–phenotype Analysis of Hearing Function in Patients with DFNB1A Caused by the C.-23+1G>A Splice Site Variant of the GJB2 Gene (Cx26)." PLoS ONE, vol. 19, no. 10, 2024, p. 1, https://doi.org/10.1371/journal.pone.0309439.